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Nine different mutations were identified.
Missense mutations were identified by Sanger sequencing (Mobix, McMaster University).
A total of 51 missense mutations were identified (Figure 1).
No point mutations were identified in invasive mucinous breast carcinoma.
Thirty CFTR mutations were identified in 24 patients (50% prevalence).
Mutations were identified most frequently in SOD1 (7.5%).
UL54 and UL97 gene mutations were identified by sequencing.
A total of 1313 mutations were identified across the 10 patient samples.
Eighty-nine mutations were identified in 41 matched pairs (PIK3CA in 27%; CDH1 in 20%).
Moreover these mutations were identified in a significant number of cases.
De novo mutations were identified in 76% of our cohort (553/732 patients; Table 2).
More suggestions(15)
mutations were detected
mutations were discovered
transfer were identified
deployment were identified
mutations were hitherto
mutations were found
mutations were selected
mutations were described
mutations were verified
mutations were eliminated
mutations were analyzed
mutations were confirmed
mutations were made
mutations were observed
mutations were created
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